...
首页> 外文期刊>European journal of gynaecological oncology >Primary adenocarcinoid tumor of the ovary arising in mature cystic teratoma. A case report.
【24h】

Primary adenocarcinoid tumor of the ovary arising in mature cystic teratoma. A case report.

机译:卵巢原发性类腺癌发生于成熟的囊性畸胎瘤。病例报告。

获取原文
获取原文并翻译 | 示例
           

摘要

Primary carcinoid tumors of the ovary are rare, forming 0.3 % of all carcinoid tumors and less than 0.1 % of ovarian malignancies. We present a case of a 47-year-old woman with abnormal vaginal bleeding and abdominal discomfort. Pelvic ultrasonography revealed a right-sided, 4 cm solid ovarian mass. At laparoscopy, a smooth surfaced, firm and mobile right adnexal mass with solid and cystic portions was detected and the tumor was excised. Pathologic and immunohistochemical examination revealed carcinoid tumor. After the evaluation of gastrointestinal and respiratory systems by imaging and endoscopic studies, no evidence of tumor tissue or metastases were found. Based on this finding, total abdominal hysterectomy, bilateral salpingo-oophorectomy, omentectomy, and appendectomy were performed and pelvic-paraaortic lymph nodes were also removed. All histological findings were similar to the features of mature cystic teratoma and carcinoid tumor. Examination of the resected lymphatic, omental and appendicealtissue indicated no tumoral invasion. Thus, the diagnosis was primary ovarian carcinoid arising from a mature cystic teratoma. This case, in the setting of a normal appendix and negative workup for an extraovarian origin, is one of a primary ovarian adenocarcinoid tumor. The primary carcinoid tumor should be differentiated from a metastatic carcinoid inside the ovary, which is always bilateral. It is important to be aware of this unusual entity in diagnoses of ovarian tumors, even in the absence of any clinical symptoms of carcinoid syndrome.
机译:卵巢原发性类癌很少见,占所有类癌的0.3%,而卵巢恶性肿瘤的发病率不到0.1%。我们介绍了一例47岁的女性,阴道异常出血,腹部不适。盆腔超声检查显示右侧有一个4厘米的卵巢实性肿块。在腹腔镜检查中,检测到具有固体和囊性部分的表面光滑,牢固和活动的右附件包块,并切除了肿瘤。病理和免疫组化检查发现类癌。在通过影像学和内窥镜检查评估胃肠道和呼吸系统后,未发现肿瘤组织或转移的证据。基于这一发现,进行了全腹子宫切除术,双侧输卵管卵巢切除术,网膜切除术和阑尾切除术,并且还去除了盆腔副主动脉淋巴结。所有组织学发现均与成熟的囊性畸胎瘤和类癌相似。对切​​除的淋巴,网膜和阑尾组织的检查表明没有肿瘤浸润。因此,诊断是由成熟的囊性畸胎瘤引起的原发性卵巢类癌。这种情况,在正常阑尾和卵巢外起源阴性检查的情况下,是原发性卵巢腺类癌的一种。原发性类癌应与卵巢内的转移类癌区分开,后者总是双侧的。重要的是要在诊断卵巢肿瘤时意识到这一异常现象,即使没有任何类癌综合征的临床症状。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号